Boretsky Karen, Hernandez Maria A, Eastburn Elizabeth, Sullivan Cornelius
Department of Anesthesia, Perioperative & Pain Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Department of Anesthesiology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Paediatr Anaesth. 2018 Mar;28(3):291-295. doi: 10.1111/pan.13328. Epub 2018 Jan 23.
The clinical reliability and reproducibility of ultrasound-guided lumbar plexus blocks is not established in pediatric populations. We present the results of a combined nerve stimulation ultrasound-guided lumbar plexus block using the vertebral body, transverse process, and psoas muscle as landmarks on a transverse lumbar paravertebral sonogram with mid-axillary transducer placement, "shamrock method," in children and adolescents.
Our primary objective was to determine the rate of achieving sensory changes in the lumbar plexus distribution. Secondary outcomes were performance time, reliability of echo-landmarks, measures of patient comfort, and complications.
We reviewed prospectively collected quality assurance data and electronic medical records of 21 patients having major orthopedic surgery with lumbar plexus block catheter for postoperative analgesia.
Twenty-one patients were studied with mean age and weight (SD, range) of 13.6 years (3.8, 6-18) and 49.3 kg (18.6, 19.2-87.6). Surgical procedures included periacetabular osteotomy, pelvic osteotomy, and proximal femoral osteotomy. Mean volume of 0.5 mL/kg (0.05) 0.2% ropivacaine produced thermal sensory changes to femoral and lateral femoral cutaneous nerves in 20/21 (95% CI 0.76 to >0.99) and 19/21 (95% CI 0.70-0.99) patients. Identification of transverse process (TP), vertebral body (VB), and psoas muscle (PM): 21/21 (95% CI 0.86-1.0). Average block performance time was 9:08 minutes (2:09, 2-13). Average opioid consumption (SD) in operating room, postanesthesia care unit, 0-12 and 12-24-hour periods were 0.17 mg/kg (0.08), 0.08 mg/kg (0.06), 0.06 mg/kg (0.06), and 0.06 mg/kg (0.05). Median pain score by severity category in postanesthesia care unit: (0-3) 66.7%, (4-6) 28.5%, (>7) 4.8%; 0-12 hours: (0-3) 76.2%, (4-6) 19.0%, (>7) 4.8%; 12-24 hours: (0-3) 57.2%, (4-6) 42.8%, (>7) 0%. No complications were recorded.
Ultrasound guidance using lateral imaging of transverse process, vertebral body, and psoas muscle allows practitioners to reach the nerves of the lumbar plexus and achieve sensory block in pediatric patients with a high success rate.
超声引导下腰丛神经阻滞在儿科人群中的临床可靠性和可重复性尚未确立。我们展示了在儿童和青少年中使用椎体、横突和腰大肌作为标志,采用腋中平面探头放置的横向腰旁超声图进行联合神经刺激超声引导下腰丛神经阻滞(“三叶草法”)的结果。
我们的主要目标是确定在腰丛神经分布区域实现感觉改变的发生率。次要结果包括操作时间、回声标志的可靠性、患者舒适度指标和并发症。
我们回顾了前瞻性收集的21例接受大型骨科手术并留置腰丛神经阻滞导管用于术后镇痛患者的质量保证数据和电子病历。
对21例患者进行了研究,平均年龄和体重(标准差,范围)分别为13.6岁(3.8,6 - 18岁)和49.3千克(18.6,19.2 - 87.6千克)。手术包括髋臼周围截骨术、骨盆截骨术和股骨近端截骨术。平均每千克体重注入0.5毫升(0.05)0.2%的罗哌卡因,使20/21(95%置信区间0.76至>0.99)和19/21(95%置信区间0.70 - 0.99)的患者股神经和股外侧皮神经出现热感觉改变。横突(TP)、椎体(VB)和腰大肌(PM)的识别率:21/21(95%置信区间0.86 - 1.0)。平均阻滞操作时间为9:08分钟(2:09,2 - 13分钟)。手术室、麻醉后监护病房、0 - 12小时和12 - 24小时期间的平均阿片类药物消耗量(标准差)分别为0.17毫克/千克(0.08)、0.08毫克/千克(0.06)、0.06毫克/千克(0.06)和0.06毫克/千克(0.05)。麻醉后监护病房按疼痛严重程度分类的中位疼痛评分:(0 - 3分)66.7%,(4 - 6分)28.5%,(>7分)4.8%;0 - 12小时:(0 - 3分)76.2%,(4 - 6分)19.0%,(>7分)4.8%;12 - 24小时:(0 - 3分)57.2%,(4 - 6分)42.8%,(>7分)0%。未记录到并发症。
利用横突、椎体和腰大肌的外侧成像进行超声引导,使从业者能够在儿科患者中成功地触及腰丛神经并实现感觉阻滞。